Canonical Allele Identifier: CA415180914

Gene: TAFAZZIN

Linked Data

• ClinVar Variation Id: 2506898
• ClinVar RCV Id: RCV003237267
• MyVariant Identifiers: chrX:g.153641819G>A (hg19) ; chrX:g.154413482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413482G>A , CM000685.2:g.154413482G>A	GRCh38
NC_000023.10:g.153641819G>A , CM000685.1:g.153641819G>A	GRCh37
NC_000023.9:g.153295013G>A	NCBI36
NG_009634.1:g.6943G>A
NG_012884.2:g.3607C>T
NG_009634.2:g.6948G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.819G>A
ENST00000698235.1:n.359G>A
ENST00000698317.1:n.1345G>A
ENST00000698318.1:n.1218G>A
ENST00000470127.2:n.563G>A
ENST00000475699.6:c.339G>A	ENSP00000419854.3:p.Trp113Ter
ENST00000476800.2:n.1471G>A
ENST00000483674.3:n.176G>A
ENST00000601016.6:c.285G>A MANE Select	ENSP00000469981.1:p.Trp95Ter
ENST00000612012.5:c.285G>A	ENSP00000482070.2:p.Trp95Ter
ENST00000612460.5:c.285G>A	ENSP00000481037.1:p.Trp95Ter
ENST00000614595.2:n.1722G>A
ENST00000615658.5:n.598G>A
ENST00000616020.5:c.339G>A	ENSP00000483636.2:p.Trp113Ter
ENST00000617701.5:c.*103G>A	ENSP00000481645.1:n.*103G>A
ENST00000621647.2:n.567G>A
ENST00000652354.1:c.9G>A	ENSP00000498734.1:p.Trp3Ter
ENST00000652358.1:c.78G>A	ENSP00000498464.1:p.Arg26=
ENST00000652390.1:c.204G>A	ENSP00000498858.1:p.Trp68Ter
ENST00000652476.1:n.675G>A
ENST00000652682.1:c.285G>A	ENSP00000498288.1:p.Trp95Ter
ENST00000652685.1:n.443G>A
ENST00000369776.8:c.210G>A	ENSP00000358791.4:p.Trp70Ter
ENST00000426231.5:c.201G>A
ENST00000439735.2:c.285G>A	ENSP00000398193.1:p.Trp95Ter
ENST00000475699.5:c.285G>A	ENSP00000419854.2:p.Trp95Ter
ENST00000476679.5:n.198G>A
ENST00000476800.1:n.392G>A
ENST00000479875.1:n.314G>A
ENST00000483780.5:n.59G>A
ENST00000601016.5:c.285G>A	ENSP00000469981.1:p.Trp95Ter
ENST00000612012.4:c.339G>A	ENSP00000482070.1:p.Trp113Ter
ENST00000612460.4:c.285G>A	ENSP00000481037.1:p.Trp95Ter
ENST00000613002.4:c.285G>A	ENSP00000478154.1:p.Trp95Ter
ENST00000613634.4:n.605G>A
ENST00000615658.4:n.698G>A
ENST00000615986.4:c.*103G>A	ENSP00000480133.1:n.*103G>A
ENST00000616020.4:c.339G>A	ENSP00000483636.1:p.Trp113Ter
ENST00000617701.4:c.*115G>A	ENSP00000481645.1:n.*115G>A
ENST00000620808.4:c.*84G>A	ENSP00000479311.1:n.*84G>A
ENST00000621647.1:n.799G>A
NM_000116.4:c.285G>A	NP_000107.1:p.Trp95Ter
NM_001303465.1:c.339G>A	NP_001290394.1:p.Trp113Ter
NM_181311.3:c.285G>A	NP_851828.1:p.Trp95Ter
NM_181312.3:c.285G>A	NP_851829.1:p.Trp95Ter
NM_181313.3:c.285G>A	NP_851830.1:p.Trp95Ter
NR_024048.2:n.717G>A
XM_006724836.1:c.339G>A	XP_006724899.1:p.Trp113Ter
XM_006724837.1:c.339G>A	XP_006724900.1:p.Trp113Ter
XM_006724839.1:c.339G>A	XP_006724902.1:p.Trp113Ter
XM_006724841.2:c.78G>A	XP_006724904.1:p.Arg26=
XM_006724842.2:c.78G>A	XP_006724905.1:p.Arg26=
XM_011531189.1:c.339G>A	XP_011529491.1:p.Trp113Ter
XM_011531190.1:c.78G>A	XP_011529492.1:p.Arg26=
XM_011531191.1:c.9G>A	XP_011529493.1:p.Trp3Ter
XM_011531192.1:c.6G>A	XP_011529494.1:p.Gly2=
XR_938511.1:n.642G>A
XM_006724841.4:c.78G>A	XP_006724904.1:p.Arg26=
XM_006724842.4:c.78G>A	XP_006724905.1:p.Arg26=
XM_011531191.2:c.9G>A	XP_011529493.1:p.Trp3Ter
XM_017029761.1:c.285G>A	XP_016885250.1:p.Trp95Ter
XM_017029762.1:c.339G>A	XP_016885251.1:p.Trp113Ter
XM_017029763.1:c.285G>A	XP_016885252.1:p.Trp95Ter
XM_017029764.1:c.6G>A	XP_016885253.1:p.Gly2=
XM_017029765.2:c.78G>A	XP_016885254.1:p.Arg26=
XM_024452431.1:c.339G>A	XP_024308199.1:p.Trp113Ter
NM_000116.5:c.285G>A MANE Select	NP_000107.1:p.Trp95Ter
NM_001303465.2:c.339G>A	NP_001290394.1:p.Trp113Ter
NM_181311.4:c.285G>A	NP_851828.1:p.Trp95Ter
NM_181312.4:c.285G>A	NP_851829.1:p.Trp95Ter
NM_181313.4:c.285G>A	NP_851830.1:p.Trp95Ter
NR_024048.3:n.696G>A